B Fowler
Overview
Explore the profile of B Fowler including associated specialties, affiliations and a list of published articles.
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Articles
175
Citations
2454
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Recent Articles
21.
Linnebank M, Lagler F, Muntau A, Roschinger W, Olgemoller B, Fowler B, et al.
J Inherit Metab Dis
. 2006 Jan;
28(6):1167-8.
PMID: 16435220
This study reports three novel mutations of the methionine adenosyltransferase (MAT) lA gene and confirms that hyperhomocysteinaemia may be a characteristic finding in MAT I/III deficiency. Thus, MAT I/III deficiency...
22.
Rea S, Kuthubutheen J, Fowler B, Wood F
Burns
. 2005 Nov;
31(8):1029-34.
PMID: 16308098
Burn injuries treated with adequate immediate first aid are associated with more favourable outcomes, limiting tissue damage and subsequent morbidity including the need for surgery. Cool running water at a...
23.
Fowler B
Ther Umsch
. 2005 Oct;
62(9):641-6.
PMID: 16218503
Over the last 20 years homocysteine has taken on increasing importance as an independent, potentially modifiable risk factor for various forms of vascular disease including peripheral and cerebral vascular disease,...
24.
Fong J, Wood F, Fowler B
Burns
. 2005 Jul;
31(5):562-7.
PMID: 15993301
In 2000 and 2002, the Royal Perth Hospital (RPH) Burn Unit, Western Australia, conducted two 'before and after' patient care audits comparing the effectiveness and cost of Silvazine (silver sulphadiazine...
25.
Baykal T, Gokcay G, Ince Z, Dantas M, Fowler B, Baumgartner M, et al.
J Inherit Metab Dis
. 2005 May;
28(2):229-33.
PMID: 15877210
A patient with a severe neonatal variant of 3-methylcrotonyl-CoA carboxylase (MCC) deficiency is reported. The first child of healthy consanguineous Turkish parents presented on the second day of life with...
26.
Stanger O, Herrmann W, Pietrzik K, Fowler B, Geisel J, Dierkes J, et al.
Z Kardiol
. 2004 Jul;
93(6):439-53.
PMID: 15252738
About half of all deaths are due to cardiovascular disease and its complications. The economic burden on society and the healthcare system from cardiovascular disability, complications, and treatments is huge...
27.
Vilaseca M, Vilarinho L, Zavadakova P, Vela E, Cleto E, Pineda M, et al.
J Inherit Metab Dis
. 2003 Sep;
26(4):361-9.
PMID: 12971424
Patients with the cblE type of homocystinuria usually present with megaloblastic anaemia, feeding difficulties, developmental delay and cerebral atrophy. We present a 14-year-old Spanish girl (patient 1) and a 10-year-old...
28.
Ramaekers V, Hansen S, Holm J, Opladen T, Senderek J, Hausler M, et al.
Neurology
. 2003 Aug;
61(4):506-15.
PMID: 12939425
Background: Previous CSF studies in Rett syndrome suggest reduced turnover of the biogenic monoamines serotonin and dopamine. Because diminished turnover may result from CNS folate depletion, the authors studied transport...
29.
Fowler B, Zeman J, Suormala T, Pristoupilova K, Kozich V, Zavadakova P
J Inherit Metab Dis
. 2003 Jan;
25(6):461-76.
PMID: 12555939
The cblE type of homocystinuria is a rare autosomal recessive disorder, which manifests with megaloblastic anaemia and developmental delay in early childhood. This disease is caused by a defect in...
30.
Litynski P, Loehrer F, Linder L, Todesco L, Fowler B
Eur J Clin Invest
. 2002 Dec;
32(9):662-8.
PMID: 12486865
Background: The 677C-->T polymorphism of methylenetetrahydrofolate reductase can lead to increased homocysteine. Moderate increases of homocysteine can be lowered by folic acid (0.4-10 mg day-1). This study compared the effect...